The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
127339331 12733933 1 I 20091110 20091110 20160912 20160912 EXP EG-ROCHE-1829044 ROCHE 61.59 YR F Y 79.00000 KG 20160912 MD EG EG

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
127339331 12733933 1 PS Trastuzumab TRASTUZUMAB 1 Intravenous (not otherwise specified) 103792 2 MG/KG SOLUTION FOR INFUSION
127339331 12733933 2 C DOCETAXEL. DOCETAXEL 1 Intravenous (not otherwise specified) 0 160 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127339331 12733933 1 HER-2 positive breast cancer
127339331 12733933 2 Breast cancer

Outcome of event

Event ID CASEID OUTC COD
127339331 12733933 LT
127339331 12733933 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127339331 12733933 Deep vein thrombosis
127339331 12733933 Dyspnoea
127339331 12733933 Pulmonary embolism

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
127339331 12733933 1 20090928 20091124 0
127339331 12733933 2 20090928 20091110 0